510(k) K071384 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901
| Applicant | Nihon Seimitsu Sokki Co., Ltd., Tachikawa-Shi, Tokyo, JP |
| Decision | Substantially Equivalent, Oct 9, 2007 |
| Received | May 17, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071384
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.